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Method to optimally select samples for validation and resequencing
BS-Seeker3: An Ultra-fast, Versatile Pipeline for Mapping Bisulfite-treated Reads.
myVCF: a web-based platform for target and exome mutations data management
Algorithm to implement Fraction and Allelic Copy number Estimate from Tumor/normal Sequencing using unmatched normal sample(s) for log ratio calculations
A tool to extract mappable reads from various library preparation protocols.
Tools for analyzing NGS sequence data and aligned protein sequences
CLAP - A pipeline used to process CLIP-seq (specifically PAR-CLIP, HITS-CLIP and iCLIP) data.
This project includes simulated and 'golden standard' datasets, software and scripts that we used to benchmark error correction tools
WOLAND is a multiplatform tool to analyze point mutation patterns using resequencing data from any organism or cell. It is implemented as a Perl and R tool using as inputs filtered unannotated or annotated SNV lists, combined with its correspondent genome sequences.
A collection of various tools useful for the deep analysis of data generated via the CRSSANT/rna2d3d pipeline.
SRSF shape analysis framework for sequencing data
pyAmpli: an amplicon-based variant filter pipeline for targeted enriched resequencing data
Program extracts a valuable information from an output vecscreen file
(Archived) This page is a record of my first formal NGS Project for Dr. Matesic of University of South Carolina (USC).
Extract unmapped read fragments from a sequence alignment map by evaluating it's concise idiosyncratic gapped alignment reports (CIGARs)
Next generation sequencing expression analysis pipeline